SOUTH SAN FRANCISCO, Calif., Oct. 02, 2019 (GLOBE NEWSWIRE)
SOUTH SAN FRANCISCO, Calif., Oct. 02, 2019 (GLOBE NEWSWIRE) -- Tempest Therapeutics, Inc., a clinical-stage biotechnology company developing a broad portfolio of first-in-class small molecules targeting diverse cancers, today announced that it will have two poster presentations at the Society for Immunotherapy of Cancer (SITC) annual meeting in National Harbor, MD.
The posters will feature Tempest’s two lead programs:
TPST-1120, a clinical stage first-in-class antagonist against peroxisome proliferator-activated receptor alpha (PPARα) that blocks a metabolic pathway required for both tumor growth and suppressive immune cells, leading to a durable anti-cancer effect.
TPST-1495, a first-in-class EP2-EP4 dual antagonist that selectively blocks prostaglandin-mediated tumor growth and immune suppression, resulting in significantly enhanced potency compared to single EP4 antagonists in clinical development.
Additionally, the company announced that Tom Dubensky, Ph.D., chief executive officer of Tempest, will be featured as an expert speaker in two conference sessions.
TPST-1495 Poster: Abstract ID P311
Dual Antagonism of Prostaglandin Receptors EP2 and EP4 by TPST-1495 Suppresses Tumor Growth and Stimulates Anti-tumor Immunity
November 8, 2019
7:00 a.m. – 8:00 p.m.
TPST-1120 Poster: Abstract ID P440
Phase 1/1b Multicenter Trial of TPST-1120, a Peroxisome Proliferator-Activated Receptor Alpha (PPARα) Antagonist as a Single Agent (SA) or in Combination in Subjects with Advanced Cancers
November 9, 2019
7:00 a.m. – 8:30 p.m.
Workshop on Intratumoral Immunomodulation Overview.
STING at a Crossroads: Untapped Potential for Innate Immunity
November 7, 2019
11:40 a.m. – 12:00 p.m.
Meet the Experts Lunch
Career Path: The Small Biotech Industry Perspective
November 7, 2019
12:00 p.m. – 1:00 p.m.
About Tempest Therapeutics Tempest Therapeutics is a clinical-stage biotechnology company advancing small molecules that modulate anti-tumor pathways with the potential to target a wide range of tumors. TPST-1120 is a first-in-class orally available small molecule which blocks the activity of a transcription factor known as PPARα, which regulates a broad set of genes required for fatty acid oxidation (FAO), a metabolic pathway. TPST-1120 has a two-pronged anti-cancer effect, inhibiting the growth of both metastatic tumors that are reliant on FAO and designated immune cell populations that prevent immune recognition and rejection of tumor cells. TPST-1120 is currently being evaluated in a Phase 1a/1b study in patients with advanced solid malignancies. TPST-1495 is a first-in-human orally available small molecule which blocks two receptors, EP2 and EP4, that bind to prostaglandin (PGE2) and initiate signaling that promotes tumor growth and proliferation of suppressive immune cell populations. Several cancer types are thought to be prostaglandin driven, including colorectal cancer, pancreatic cancer, and head and neck cancer. Signaling through both EP2 and EP4 has been shown to promote tumor growth. In preclinical studies, TPST-1495 has significantly increased potency compared to single EP4 antagonists in clinical development. Tempest anticipates evaluating TPST-1495 in patients with advanced cancers in early 2020.
Tempest, headquartered in South San Francisco, is supported by key healthcare investors, including Versant Ventures, F-Prime Capital, Quan Capital, Lilly Asia Ventures, Foresite Capital and Eight Roads Ventures. More information about Tempest can be found on the company’s website at www.tempesttx.com.
"Featured Content" profiles are meant to provide awareness of these companies to investors in the small-cap and growth equity community and should not in any way come across as a recommendation to buy, sell or hold these securities. BiomedReports is not paid or compensated by newswires to disseminate or report news and developments about publicly traded companies, but may from time to time receive compensation for advertising, data, analytics and investor relation services from various entities and firms. Full disclosures should be read in the 'About Us Section'. Add this page to your favorite Social Bookmarking websites